G69V (p.Gly69Val) variant of CYP17A1 (P05093)
G69V (p.Gly69Val) in CYP17A1 (P05093) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G69V (p.Gly69Val) variant details
- p.Gly69Val
- NCI-TCGA Cosmic COSV1008
- cosmic curated COSV10088
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available